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1.
J Cytol ; 39(1): 20-25, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-35341111

RESUMEN

Context: Sentinel lymph node (SLN) biopsy is the standard of care for breast cancer (BC) patient staging. The axillary node status can be evaluated by frozen section (FS) or imprint cytology (IC). Despite the major disadvantages of tissue loss and freezing artifact in FS, many pathologists consider SLN IC a more difficult task requiring special expertise and prefer FS to IC. Aims: To conduct a large cohort study to evaluate the results of intraoperative SLN IC, compare them with those of FS and permanent section (PS), and determine the best method for general pathologists. Settings and Design: A very large cohort study with many pathologists engaged was designed and the diagnostic results were compared. Materials and Methods: With 12 pathologists engaged, we conducted the largest patient cohort study of SLN IC to date, including 4,327 consecutive BC patients undergoing SLN biopsy during the past 15 years. The touch imprints were stained using three different methods and evaluated. The PS was used as the gold standard for evaluation. Statistical Analysis: The false positivity, false negativity, accuracy, sensitivity, and specificity of the IC and FS for each pathologist were evaluated and compared. Results: Our results showed an overall sensitivity of 82.7%, specificity of 99.3%, and an accuracy rate of 95.9% for SLN IC, which were comparable to those of FS. The accuracy rate did not correlate with the length of working experience and the staining method. Conclusions: Intraoperative hematoxylin and eosin (H&E)-stained IC preparation was found to be the best SLN examination method for general pathologists.

2.
J Am Podiatr Med Assoc ; 111(4)2021 Jul 01.
Artículo en Inglés | MEDLINE | ID: mdl-34478538

RESUMEN

Subungual schwannoma is quite rare and often causes nail deformity and difficulty in wearing shoes. Complete tumor excision is the treatment of choice, and we advocate that restoring the nail appearance should be considered at the same time. We present the case of 43-year-old man with a big toe subungual schwannoma. We designed a zigzag incision method to excise the tumor and also corrected nail-bed deformity. The patient had a smooth recovery, and the nail plate regrew with a good appearance.


Asunto(s)
Hallux , Enfermedades de la Uña , Neurilemoma , Adulto , Humanos , Masculino , Enfermedades de la Uña/cirugía , Uñas , Neurilemoma/complicaciones , Neurilemoma/cirugía , Colgajos Quirúrgicos
3.
World J Gastroenterol ; 24(38): 4412-4418, 2018 Oct 14.
Artículo en Inglés | MEDLINE | ID: mdl-30344425

RESUMEN

Gastric polyposis is a rare disease. Not all polyps progress to cancer. Monoallelic mutation in Fanconi anemia (FA) genes, unlike biallelic gene mutations that causes typical FA phenotype, can increase risks of cancers in a sporadic manner. Aberrations in the FA pathway were reported in all molecular subtypes of gastric cancer. We studied a patient with synchronous gastric cancer from gastric polyposis by conducting a 13-year long-term follow up. Via pathway-driven massive parallel genomic sequencing, a germline mutation at FANCA D1359Y was identified. We identified several recurrent mutations in DNA methylation (TET1, V873I), the ß-catenin pathway (CTNNB1, S45F) and RHO signaling pathway (PLEKHG5, R203C) by comparing the genetic events between benign and malignant gastric polyps. Furthermore, we revealed gastric polyposis susceptible genes and genetic events promoting malignant transformation using pathway-driven targeted gene sequencing.


Asunto(s)
Pólipos Adenomatosos/genética , Proteína del Grupo de Complementación A de la Anemia de Fanconi/genética , Predisposición Genética a la Enfermedad , Neoplasias del Yeyuno/genética , Neoplasias Gástricas/genética , Pólipos Adenomatosos/complicaciones , Pólipos Adenomatosos/diagnóstico por imagen , Pólipos Adenomatosos/patología , Anciano , Anemia Ferropénica/etiología , Biopsia , Análisis Mutacional de ADN , Gastrectomía , Hemorragia Gastrointestinal/etiología , Gastroscopía , Humanos , Neoplasias del Yeyuno/diagnóstico por imagen , Neoplasias del Yeyuno/patología , Neoplasias del Yeyuno/cirugía , Yeyuno/diagnóstico por imagen , Yeyuno/patología , Yeyuno/cirugía , Masculino , Mutación , Estómago/diagnóstico por imagen , Estómago/patología , Estómago/cirugía , Neoplasias Gástricas/complicaciones , Neoplasias Gástricas/diagnóstico por imagen , Neoplasias Gástricas/patología , Neoplasias Gástricas/cirugía , Tomografía Computarizada por Rayos X
4.
Mol Carcinog ; 55(5): 499-513, 2016 May.
Artículo en Inglés | MEDLINE | ID: mdl-25728212

RESUMEN

Growth differentiation factor-10 (GDF10), commonly referred as BMP3b, is a member of the transforming growth factor-ß (TGF-ß) superfamily. GDF10/BMP3b has been considered as a tumor suppressor, however, little is known about the molecular mechanism of its roles in tumor suppression in oral cancer. Clinical significance of GDF10 downregulation in oral squamous cell carcinoma (OSCC) was evaluated using three independent cohorts of OSCC patients. The molecular mechanisms of GDF10 in the suppression of cell survival, cell migration/invasion and epithelial-mesenchymal transition (EMT) were investigated by using oral cancer cell lines. The present study shows that GDF10 is downregulated during oral carcinogenesis, and GDF10 expression is also an independent risk factor for overall survival of OSCC patients. Overexpression of GDF10 attenuates cell proliferation, transformation, migration/invasion, and EMT. GDF10-inhibited EMT is mediated by ERK signaling but not by typical TGF-ß signaling. In addition, overexpression of GDF10 promotes DNA damage-induced apoptosis and sensitizes the response to all-trans retinoic acid (ATRA) and camptothecin (CPT). Intriguingly, the expression of GDF10 is induced by type III TGF-ß receptor (TGFBR3) through TGF-ß-SMAD2/3 signaling. Our findings suggest that TGFBR3 is an upstream activator of GDF10 expression and they share the same signaling to inhibit EMT and migration/invasion. These results support that GDF10 acts as a hinge to collaborate with TGFBR3 in the transition of EMT-MET program. Taken together, we illustrated the clinical significance and the molecular mechanisms of tumor-suppressive GDF10 in OSCC.


Asunto(s)
Carcinoma de Células Escamosas/patología , Resistencia a Antineoplásicos , Transición Epitelial-Mesenquimal , Factor 10 de Diferenciación de Crecimiento/metabolismo , Neoplasias de la Boca/patología , Proteoglicanos/metabolismo , Receptores de Factores de Crecimiento Transformadores beta/metabolismo , Carcinoma de Células Escamosas/tratamiento farmacológico , Carcinoma de Células Escamosas/genética , Carcinoma de Células Escamosas/metabolismo , Línea Celular Tumoral , Movimiento Celular , Proliferación Celular , Regulación hacia Abajo , Regulación Neoplásica de la Expresión Génica , Factor 10 de Diferenciación de Crecimiento/genética , Humanos , Neoplasias de la Boca/tratamiento farmacológico , Neoplasias de la Boca/genética , Neoplasias de la Boca/metabolismo , Pronóstico , Proteoglicanos/genética , Receptores de Factores de Crecimiento Transformadores beta/genética , Análisis de Supervivencia
5.
Int J Surg Pathol ; 22(6): 536-9, 2014 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-24448019

RESUMEN

Primary salivary gland-type lung cancers are a rare group of tumors. When they do occur, the most common type is adenoid cystic carcinoma, followed by mucoepidermoid carcinoma. Primary high-grade salivary-type duct carcinoma (HGSDC) arising in the lung has not been described. We report a case of primary pulmonary HGSDC in a 55-year-old woman who was referred to our hospital for a suspicious lung tumor. The chest computed tomography revealed a solid mass in the left upper lobe. A lobectomy was performed afterward, and the mass was a primary lung HGSDC. To the best of our knowledge, HGSDC arising in the lung has not been reported previously.


Asunto(s)
Carcinoma Ductal/patología , Neoplasias Pulmonares/patología , Glándulas Salivales/patología , Biomarcadores de Tumor/análisis , Femenino , Humanos , Inmunohistoquímica , Persona de Mediana Edad , Clasificación del Tumor
6.
Tumour Biol ; 34(5): 2557-64, 2013 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-23625657

RESUMEN

hPuf-A is a member of RNA-binding PUF family that regulates mRNA translation. Redistribution of hPuf-A from the nucleolus to the nucleoplasm upon genotoxic stress modulates the poly(ADP-ribosyl)ation activity of PARP-1. Here, we report a novel function of hPuf-A involved in promoting breast cancer progression. Immunohistochemical studies showed higher expression levels of hPuf-A in stage I, II, III, and IV breast cancer specimens in contrast with those of hPuf-A in ductal carcinoma in situ. The presence of hPuf-A is highly associated with colony formation capacities in breast cancer T47D and MDA-MB-231 cells. Xenograft growth of hPuf-A-silenced and hPuf-A overexpressing MDA-MB-231 cells in nude mice was substantially in concert with colony formation capacities. This promoting effect of hPuf-A in tumorigenesis might be correlated with the regulation of its associated mRNAs, such as RbAp48 and DDX3. Collectively, hPuf-A may have diagnostic values in breast cancer progression.


Asunto(s)
Neoplasias de la Mama/metabolismo , Carcinogénesis/metabolismo , Carcinoma Intraductal no Infiltrante/metabolismo , Neoplasias Pulmonares/metabolismo , Proteínas de Unión al ARN/genética , Animales , Neoplasias de la Mama/patología , Carcinogénesis/patología , Carcinoma Intraductal no Infiltrante/secundario , Línea Celular Tumoral , Femenino , Expresión Génica , Regulación Neoplásica de la Expresión Génica , Humanos , Neoplasias Pulmonares/secundario , Ratones , Ratones Endogámicos BALB C , Ratones Desnudos , Antígenos de Histocompatibilidad Menor , Estadificación de Neoplasias , Trasplante de Neoplasias , Proteínas de Unión al ARN/metabolismo , Carga Tumoral , Regulación hacia Arriba
8.
Am J Otolaryngol ; 32(6): 620-3, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21168242

RESUMEN

Sebaceous gland carcinoma (SGC) of the eyelid is a highly malignant neoplasm that arises from the meibomian glands, glands of Zeis, and sebaceous glands of the skin. The characteristics of this disease are high recurrence rate, significant metastatic potential, and notable mortality rate, which are quite different from basal cell carcinoma (BCC). We report the case of a 37-year-old woman with the history of left lower eyelid BCC (diagnosed 9 years ago), who had left parotid lymph nodes metastases and local recurrence twice. The chief complaint during visit was a left upper eyelid swelling mass noted for 3 months. She received salvage ablation surgery later. The final pathologic report is SGC. The diagnosis corresponds to the clinical presentation of this patient at last. The delay between initial examination and final diagnosis in this patient is about 9 years, but operation and concurrent chemotherapy and radiotherapy were performed after left parotid lymph nodes metastasis was noted. Although there was still local recurrence after concurrent chemotherapy and radiotherapy, the patient is still alive without distant metastasis. In this article, we would discuss the differences of the pathologic characters, treatment, and prognosis between SGC and BCC.


Asunto(s)
Adenocarcinoma Sebáceo/patología , Carcinoma Basocelular/patología , Neoplasias de los Párpados/patología , Ganglios Linfáticos/patología , Recurrencia Local de Neoplasia/patología , Neoplasias de las Glándulas Sebáceas/patología , Adenocarcinoma Sebáceo/diagnóstico , Adenocarcinoma Sebáceo/cirugía , Adulto , Biopsia con Aguja , Carcinoma Basocelular/diagnóstico , Carcinoma Basocelular/cirugía , Diagnóstico Diferencial , Neoplasias de los Párpados/diagnóstico , Neoplasias de los Párpados/cirugía , Femenino , Estudios de Seguimiento , Humanos , Inmunohistoquímica , Invasividad Neoplásica/patología , Recurrencia Local de Neoplasia/diagnóstico , Recurrencia Local de Neoplasia/cirugía , Estadificación de Neoplasias , Medición de Riesgo , Neoplasias de las Glándulas Sebáceas/diagnóstico , Neoplasias de las Glándulas Sebáceas/cirugía , Factores de Tiempo , Resultado del Tratamiento
9.
Pathology ; 42(2): 147-50, 2010 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-20085516

RESUMEN

AIMS: To determine risk factors for recurrence of desmoid-type fibromatosis (aggressive fibromatosis). METHODS: Forty-six cases of desmoid-type fibromatosis in Taiwanese patients were analysed for an association between tumour recurrence and clinical features, pathology, and the presence of p53 protein and beta-catenin on immunohistochemical staining. RESULTS: Six (13%) of 46 patients developed recurrence after surgical resection. The only factor significantly associated with tumour recurrence was positive surgical margin (p = 0.035). CONCLUSIONS: A positive surgical margin is a risk factor for recurrence of desmoid-type fibromatosis.


Asunto(s)
Fibromatosis Abdominal/patología , Fibromatosis Agresiva/patología , Adulto , Biomarcadores de Tumor/metabolismo , Femenino , Fibromatosis Abdominal/metabolismo , Fibromatosis Abdominal/cirugía , Fibromatosis Agresiva/metabolismo , Fibromatosis Agresiva/cirugía , Humanos , Inmunohistoquímica , Masculino , Recurrencia Local de Neoplasia , Pronóstico , Factores de Riesgo , Proteína p53 Supresora de Tumor/metabolismo , beta Catenina/metabolismo
10.
Surgery ; 147(6): 847-53, 2010 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-20045163

RESUMEN

BACKGROUND: Epidemiologic studies have shown that obesity is associated with an increased risk of thyroid cancer. Leptin, an adipocyte-derived cytokine, can act as a growth factor on certain normal and transformed cells. Aberrant expression of leptin or leptin receptor has been detected in some types of cancer. The aim of this study is to determine immunohistochemical expression of leptin and leptin receptor in papillary thyroid cancer to investigate the relationship between their expression and clinicopathologic features. METHODS: The expression of leptin and leptin receptor was assessed in 49 primary neoplasms and 15 lymph node metastases using a semiquantitative immunohistochemical staining method. RESULTS: Leptin and leptin receptor were expressed in 37% and 51% of papillary thyroid cancer, respectively. They were not expressed in normal follicles. In the primary neoplasms and the metastatic nodes, expression of leptin correlated closely with leptin receptor (P < .001 for the primary neoplasms and P = .017 for nodal metastases). Expression of either protein was associated with greater neoplasm size (leptin expression, 32.0 +/- 10.7 vs 20.5 +/- 8.4 mm; P = .001; leptin receptor expression, 27.9 +/- 11.5 vs 21.4 +/- 9.0 mm; P = .032). Coexpression of leptin and leptin receptor in primary neoplasms had greater incidence of lymph node metastasis (P = .038). CONCLUSION: Expression of leptin and/or leptin receptor in papillary thyroid cancer is associated with neoplasm aggressiveness, including tumor size and lymph node metastasis.


Asunto(s)
Carcinoma Papilar/genética , Carcinoma Papilar/cirugía , Leptina/genética , Receptores de Leptina/genética , Neoplasias de la Tiroides/genética , Neoplasias de la Tiroides/cirugía , Adulto , Índice de Masa Corporal , Carcinoma Papilar/metabolismo , Carcinoma Papilar/patología , Femenino , Humanos , Inmunohistoquímica , Leptina/metabolismo , Metástasis Linfática/genética , Metástasis Linfática/patología , Masculino , Persona de Mediana Edad , Receptores de Leptina/metabolismo , Neoplasias de la Tiroides/metabolismo , Neoplasias de la Tiroides/patología
12.
Kaohsiung J Med Sci ; 25(12): 663-8, 2009 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-19951852

RESUMEN

We report a patient with congenital generalized lipodystrophy who had suffered from seizures, myoclonus, ataxia and cognitive decline since late childhood. Lafora disease was diagnosed based on skin biopsy results, which revealed pathognomonic Lafora bodies. The results of genetic analysis for mutations in EPM2A and EPM2B genes were negative. This is the first case report describing an association between congenital generalized lipodystrophy and Lafora disease. Further studies focusing on the relationship between these two diseases and the identification of a third locus for Lafora disease are needed.


Asunto(s)
Enfermedad de Lafora/complicaciones , Lipodistrofia/congénito , Proteínas Portadoras/genética , Niño , Humanos , Enfermedad de Lafora/genética , Lipodistrofia/complicaciones , Lipodistrofia/genética , Masculino , Proteínas Tirosina Fosfatasas no Receptoras/genética , Ubiquitina-Proteína Ligasas
14.
Langenbecks Arch Surg ; 393(5): 729-32, 2008 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-18404277

RESUMEN

BACKGROUND: The likelihood of thyroid cancer is similar in patients with one or more nodules, but tumor characteristics of thyroid cancer in glands with multinodular goiter are unclear. MATERIALS AND METHODS: This study consisted of 100 consecutive patients (ages 15-81 years; 84 women), who underwent thyroidectomy for papillary or follicular thyroid carcinoma between 2005 and 2006. Patient demographics, diagnostic tests, operations, and pathological findings were reviewed. RESULTS: In a univariate analysis, cancer diagnosed within multinodular goiter was different from solitary cancer nodule in age of diagnosis (48 vs 40 years, p = 0.002), tumor size (1.42 vs 2.20 cm, p = 0.024), and the presence of cervical lymph node metastases (p = 0.035). There was no difference in gender, extrathyroidal invasion, multifocality, and types of operation. Only age (odds ratio, 1.056) and tumor size (odds ratio, 0.730) revealed independent correlation in multivariate analysis. CONCLUSION: Thyroid cancer in glands with multiple nodules is associated with older age at diagnosis and smaller tumor size.


Asunto(s)
Adenocarcinoma Folicular/patología , Carcinoma Papilar/patología , Bocio Nodular/patología , Neoplasias de la Tiroides/patología , Adenocarcinoma Folicular/cirugía , Adolescente , Adulto , Factores de Edad , Anciano , Anciano de 80 o más Años , Carcinoma Papilar/cirugía , Femenino , Bocio Nodular/cirugía , Humanos , Metástasis Linfática , Masculino , Persona de Mediana Edad , Invasividad Neoplásica , Estadística como Asunto , Glándula Tiroides/patología , Neoplasias de la Tiroides/cirugía , Tiroidectomía , Adulto Joven
15.
Abdom Imaging ; 32(6): 701-4, 2007 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-17632752

RESUMEN

The purpose of this study was to evaluate the presence of the hyperdense appendix in acute appendicitis. The CT scans of 183 patients with pathologically proven acute appendicitis were reviewed to determine the prevalence of a hyperdense appendix, defined as a high-attenuated appendix when compared with the adjacent cecal wall on precontrast CT. A control group consisted of 100 patients with CT examinations performed in the emergency department were also randomly allocated to search for any hyperdense appendix in other disease conditions. The images were reviewed by two radiologists who reached a decision by consensus. A hyperdense appendix sign was found in 61 of 183 (33%) patients, including 92 men and 91 women ranging in age from 17 to 85 years (mean 37 years). On the other hand, the sign was seen in only two (2%) of the 88 patients in whom appendicitis was not diagnosed. The hyperdense appendix sign on unenhanced CT is seen in about 33% of patients with acute appendicitis. The false-positive rate is very low, rendering it a very useful sign for diagnosis of acute appendicitis.


Asunto(s)
Apendicitis/diagnóstico por imagen , Tomografía Computarizada por Rayos X/métodos , Enfermedad Aguda , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Apendicitis/patología , Distribución de Chi-Cuadrado , Diagnóstico Diferencial , Servicio de Urgencia en Hospital , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos
16.
Dig Dis Sci ; 52(3): 792-7, 2007 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-17253141

RESUMEN

The aim of this study is to estimate the incidence of the gastrointestinal stromal tumor after the previous diagnoses were confirmed and/or revised by both immunohistochemical and mutational analyses. We reviewed 17,858 surgically excised gastrointestinal lesions in our hospital from 1998 to 2004. All mesenchymal tumors were examined for CD117 expression by immunohistochemistry, and every CD117-negative mesenchymal tumors were further subjected to mutational analysis for KIT and PDGFRA exons. The results showed that approximately 35% of gastrointestinal stromal tumors were misdiagnosed if immunohistochemical analysis of CD117 expression was not performed; and approximately 15% misdiagnosed if mutation analysis was not available. Because approximately 4.72% of patients with gastrointestinal malignancies in Taiwan were treated in our hospital and the average of newly diagnosed gastrointestinal stromal tumors in our hospital was 14.33 cases per year, the estimated annual incidents of gastrointestinal stromal tumor in Taiwan were 303.60. Therefore, the annual incidence of gastrointestinal stromal tumor is 13.74 per million Taiwanese.


Asunto(s)
Tumores del Estroma Gastrointestinal/epidemiología , Neoplasias del Apéndice/sangre , Neoplasias Colorrectales/sangre , Neoplasias Colorrectales/epidemiología , Análisis Mutacional de ADN , Neoplasias Esofágicas/sangre , Neoplasias Esofágicas/epidemiología , Tumores del Estroma Gastrointestinal/sangre , Humanos , Inmunohistoquímica , Incidencia , Proteínas Proto-Oncogénicas c-kit/sangre , Receptor alfa de Factor de Crecimiento Derivado de Plaquetas/sangre , Estudios Retrospectivos , Neoplasias Gástricas/sangre , Neoplasias Gástricas/epidemiología , Taiwán/epidemiología
17.
World J Surg ; 30(8): 1414-21, 2006 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-16865317

RESUMEN

INTRODUCTION: Phyllodes tumors of the breast are uncommon, and it is difficult to predict biologic behavior based on clinicopathologic features. Despite the wealth of data on the factors to predict recurrence, little is known about the impact of treatment refinements. This study seeks to define changes in patient characteristics, histopathologic parameters, and outcome between the two periods before and after the care of patients with breast diseases was centralized to a breast specialty. METHODS: The records of 182 patients with phyllodes tumors managed surgically were reviewed. Patients treated from 1985 to 1996 (n=81) were compared with those seen from 1997 to 2004 (n=101). RESULTS: The analysis of the two treatment periods revealed that there was a decrease in tumor size at diagnosis, from 7.7 cm during the earlier period to 4.6 cm during the recent period (P=0.003). The patients undergoing breast-conserving surgery were significantly increased during the recent period. In contrast, pathologic features and local recurrence rates remained unchanged during the study period. Multivariate analysis revealed that positive surgical margin was the only independent predictor of recurrence, with an increased hazard of 8.0. Overall, upgrading to the next grade was observed in 16% of recurrences. CONCLUSIONS: Breast-conserving surgery with clear margins is the current treatment of choice for phyllodes tumors, but this strategy does not further reduce local recurrence effectively. Optimal management continues to be a challenge.


Asunto(s)
Neoplasias de la Mama/cirugía , Tumor Filoide/cirugía , Adolescente , Adulto , Anciano , Niño , Femenino , Humanos , Mastectomía , Persona de Mediana Edad , Recurrencia Local de Neoplasia
18.
J Formos Med Assoc ; 105(4): 290-8, 2006 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-16618609

RESUMEN

BACKGROUND: The role of mycobacterial infection, particularly related to Mycobacterium avium subsp paratuberculosis (Map), in Crohn's disease has long been debated. We developed primer pairs capable of detecting a broad spectrum of mycobacterium and employed them to investigate surgical specimens from patients with Crohn's disease. METHODS: Pan mycobacterium primers of the 65-kDa heat shock protein gene (Hsp65) were used in a polymerase chain reaction (PCR) to examine 12 surgically-resected, formalin-fixed, paraffin-embedded specimens from 11 patients with Crohn's disease. The DNA sequences of amplicons were aligned with those in GenBank. RESULTS: Mycobacterial DNA was found in specimens from three of 11 patients. M. mucogenicum was identified in a specimen from one patient and M. tuberculosis in two, but Map was not identified in any. CONCLUSION: Hsp65-based PCR can be employed to search for occult mycobacterial infection of the gastrointestinal tract in patients with a diagnosis or suspicion of Crohn's disease. This approach may have a therapeutic implication.


Asunto(s)
Enfermedad de Crohn/microbiología , ADN Bacteriano/análisis , Mycobacterium/aislamiento & purificación , Reacción en Cadena de la Polimerasa/métodos , Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Homología de Secuencia de Ácido Nucleico
20.
Ann Thorac Cardiovasc Surg ; 12(6): 428-31, 2006 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-17228283

RESUMEN

Constrictive pericarditis (CP) following hemopericardium has been reported in the literature but its pathogenesis is open to question. Proposed mechanisms include trauma leading to damage of the mesothelial lining resulting in decreased fibrinolytic activity in the presence of blood. We present a patient who sustained blunt thoracoabdominal trauma in a car accident and subsequently developed delayed hemopericardium leading to constrictive pericarditis and impending cardiac tamponade. We performed a pericardiectomy to relieve the compression. Closely prolonged monitoring and emergent operation are suggested for such kinds of delayed complications.


Asunto(s)
Lesiones Cardíacas/complicaciones , Derrame Pericárdico/cirugía , Pericarditis Constrictiva/cirugía , Heridas no Penetrantes/complicaciones , Adulto , Lesiones Cardíacas/cirugía , Humanos , Masculino , Derrame Pericárdico/diagnóstico , Derrame Pericárdico/etiología , Pericardiectomía , Pericarditis Constrictiva/diagnóstico , Pericarditis Constrictiva/etiología
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